Canonical Allele Identifier: PA103958
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 156
ClinVar RCV Id: RCV000000179 RCV002509140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000265.1:p.Leu402Pro
CA113940
NM_000274.4:c.1205T>C